The study aims to evaluate the therapeutic effects of the dual-target, task-integrated rTMS intervention on post-stroke aphasia and motor dysfunction.
Conditions
Interventions
sham TMS group:placebo stimulation
Treatment Group:Dual-target rTMS
Control Group:Single Target rTMS
Sponsors
Affiliated Hospital of Hangzhou Normal University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Diagnosed with stroke according to the Chinese Guidelines for the Diagnosis and Treatment of Cerebral Haemorrhage (2019) or the Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke (2018); 2. First-time onset with stable condition; 3. Native Chinese speaker with normal language and motor function prior to onset; 4. Diagnosed with aphasia, right-handed.
Exclusion criteria
Exclusion criteria: 1. Individuals with unstable vital signs and severe underlying medical conditions; 2. History of stroke, neurological or psychiatric disorders, alcoholism, or substance abuse; 3. Presence of metallic implants, electronic devices, or cranial defects; 4. Severe articulation disorders; 5. Concurrent severe dysfunction of vital organs such as heart, lungs, or liver; 6. Refusal to participate in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cognitive Behaviour;life skills;brain function; | — |
Countries
China
Contacts
Public ContactZhang Ye
Affiliated Hospital of Hangzhou Normal University
Outcome results
None listed